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Multimodal-based Real-world Single-center Retrospective Observational Study on Full-process Intelligent Management of Osteoporosis

Multimodal-based Real-world Single-center Retrospective Observational Study on Full-process Intelligent Management of Osteoporosis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116921
Enrollment
Unknown
Registered
2026-01-16
Start date
2026-01-29
Completion date
Unknown
Last updated
2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoporosis

Interventions

Intelligent Intervention Group:NA
Regular Management Team:NA

Sponsors

The First Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with osteoporosis through computerized multimodal fusion; 2. Age >= 40 years; 3. Data from November 2020 to November 2025.

Exclusion criteria

Exclusion criteria: 1. Patients with severe cognitive impairments (such as advanced Alzheimer's disease), mental disorders (such as acute schizophrenia), who cannot cooperate to complete bone density tests, questionnaires, and follow-ups. 2. Patients with advanced malignant tumors (such as stage IV cancer with extensive metastasis) or severe liver and kidney failure (such as decompensated liver cirrhosis, uremia dialysis dependence), with an expected survival period of less than 6 months, and unable to complete at least one follow-up. 3. Patients who have recently suffered a severe fracture (such as femoral neck fracture, vertebral compression fracture) and are in a bedridden and immobilized state, and are temporarily unable to undergo bone density tests or rehabilitation assessment. 4. Patients who are allergic to the contrast agent used in bone density tests, or who cannot cooperate to complete DXA tests due to physical deformities (such as severe scoliosis). 5. Patients who cannot cooperate with robotic surgery or rehabilitation robot training (such as severe joint deformities, neurological dysfunction, etc.).

Design outcomes

Primary

MeasureTime frame
Accuracy Rate (ACC);Sensitivity (SEN / Recall Rate);Specificity (SPE);

Secondary

MeasureTime frame
Decision Curve Analysis (DCA);

Countries

China

Contacts

Public ContactHuilin Yang

The First Affiliated Hospital of Soochow University

154141733@qq.com+86 166 0512 8900

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026